Progression of Follicular Thyroid Carcinomas to Anaplastic Thyroid Carcinomas: Molecular and Clinicopathologic Characteristics with Comparison to Papillary Thyroid Carcinoma-Derived Anaplastic Thyroid Carcinomas.

IF 4.6 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Toru Odate, Tetsuo Kondo, Ryohei Katoh, Koichi Ito, Toshihide Ueno, Yasushi Yatabe, Taisuke Mori
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引用次数: 0

Abstract

Although anaplastic thyroid carcinomas (ATCs) typically arise from papillary thyroid carcinomas (PTCs), follicular thyroid carcinomas (FTCs) can also progress to ATCs; however, histologically confirmed FTC-derived ATCs are relatively uncommon and remain poorly characterized. To clarify this phenomenon, we analyzed eight FTC-derived ATCs and compared them with 11 PTC-derived ATCs. Whole-exome sequencing (WES) was conducted on the differentiated thyroid carcinoma (DTC) and ATC components within the same tumors to examine mutational profiles; three additional cases underwent FoundationOne® testing. The demographic features were similar between FTC- and PTC-derived ATCs. Histologically, spindle-cell morphology was more common in FTC-derived ATCs (3/8), whereas PTC-derived ATCs exhibited squamoid (5/11) and giant cell features (5/11), including osteoclast-like cells. WES was successfully performed on both the ATC and FTC components in seven of the eight FTC-derived ATCs. Common alterations included TERT promoter (5/7), NRAS (4/7), and HRAS (2/7) mutations in both components. TP53 mutations were observed only in the ATC component (5/7). EIF1AX mutations co-occurred with TERT and HRAS mutations in two cases. PTEN mutations were found in two FTCs with solid/trabecular patterns but were absent in the corresponding ATC components. One tumor harbored a DGCR8 p.E518K mutation that was retained during progression. By contrast, PTC-derived ATCs consistently showed concurrent BRAF and TERT promoter mutations (11/11). Immunohistochemistry for BRAF V600E, RAS Q61R, p53, PTEN, and MTAP showed high concordance with the corresponding mutation status. These findings revealed significant histological and genetic differences between FTC- and PTC-derived ATCs, providing new insights into the molecular basis of FTC dedifferentiation into ATC.

滤泡性甲状腺癌向间变性甲状腺癌的进展:分子和临床病理特征与乳头状甲状腺癌衍生的间变性甲状腺癌的比较。
虽然间变性甲状腺癌(ATCs)通常起源于乳头状甲状腺癌(ptc),但滤泡性甲状腺癌(FTCs)也可以发展为ATCs;然而,组织学证实的ftc来源的ATCs相对不常见,特征仍然很差。为了澄清这一现象,我们分析了8个ftc衍生的ATCs,并将它们与11个ptc衍生的ATCs进行了比较。对同一肿瘤中的分化型甲状腺癌(DTC)和ATC成分进行全外显子组测序(WES)以检测突变谱;另外3例患者接受了FoundationOne®检测。FTC和ptc衍生ATCs的人口统计学特征相似。组织学上,纺锤细胞形态在ftc来源的ATCs中更为常见(3/8),而ptc来源的ATCs表现出鳞状(5/11)和巨细胞特征(5/11),包括破骨细胞样细胞。在8个FTC衍生的ATC中,有7个在ATC和FTC组件上成功地进行了WES。常见的改变包括TERT启动子(5/7)、NRAS(4/7)和HRAS(2/7)突变。仅在ATC组分中观察到TP53突变(5/7)。2例EIF1AX突变与TERT和HRAS突变同时发生。PTEN突变在两个实心/小梁型的FTCs中发现,但在相应的ATC成分中不存在。一种肿瘤携带DGCR8 p.E518K突变,该突变在进展过程中保留。相比之下,ptc衍生的ATCs一致显示BRAF和TERT启动子同时突变(11/11)。BRAF V600E、RAS Q61R、p53、PTEN和MTAP的免疫组化与相应的突变状态高度一致。这些发现揭示了FTC和ptc衍生的ATCs在组织学和遗传学上的显著差异,为FTC去分化为ATC的分子基础提供了新的见解。
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来源期刊
Endocrine Pathology
Endocrine Pathology 医学-病理学
CiteScore
12.30
自引率
20.50%
发文量
41
审稿时长
>12 weeks
期刊介绍: Endocrine Pathology publishes original articles on clinical and basic aspects of endocrine disorders. Work with animals or in vitro techniques is acceptable if it is relevant to human normal or abnormal endocrinology. Manuscripts will be considered for publication in the form of original articles, case reports, clinical case presentations, reviews, and descriptions of techniques. Submission of a paper implies that it reports unpublished work, except in abstract form, and is not being submitted simultaneously to another publication. Accepted manuscripts become the sole property of Endocrine Pathology and may not be published elsewhere without written consent from the publisher. All articles are subject to review by experienced referees. The Editors and Editorial Board judge manuscripts suitable for publication, and decisions by the Editors are final.
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